Polymorphs of deuterated omega-diphenylurea or salts thereof

ABSTRACT

The invention relates to polymorphs of deuterated omega-diphenylurea or salts thereof. In particular, the invention provides polymorphs of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide or its salt, namely, polymorphs of the compound as shown in formula (I) or its salt. The polymorphs are suited for preparing the pharmaceutical composition used for inhibiting phosphokinase (such as raf kinases).

TECHNICAL FIELD

The present invention relates to the field of medicine, and particularly, relates to polymorphs of deuterated omega-diphenylurea or salts thereof, and more particularly, relates to polymorphs of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide or salts thereof.

BACKGROUND

The structure of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide is shown as formula I.

The compound of formula I, with a molecular formula of C₂₁H₁₃D₃ClF₃N₄O₃ and a molecular weight of 467.84, is a white or off-white crystal powder, odorless and tasteless. It is very soluble in dimethyl sulfoxide or dimethyl formamide, sparingly soluble in methanol, slightly soluble in acetone, anhydrous ethanol and glacial acetic acid, and practically insoluble in water.

The compound of formula I belongs to compounds that inhibit raf kinase, and is suitable for preparing drugs for the treatment of cancer and other related diseases. Different crystal forms of a drug might affect its dissolution, absorption in vivo, thereby affecting its clinical therapeutic effect and safety to a certain extent. In particular, for some slightly soluble solid or semisolid oral preparations, the influence of crystal forms is huge. There are no studies on polymorphs of compound I up to now, and no polymorphs of compound I have been developed yet.

Therefore, it is necessary to develop the polymorphs of compound I.

SUMMARY OF INVENTION

The purpose of the present invention is to provide polymorphs of compound I or pharmaceutically acceptable salts thereof, or solvates thereof.

In the first aspect, polymorphs of compound I or pharmaceutically acceptable salts thereof, or solvates thereof is provided,

In another embodiment, the pharmaceutically acceptable salt is a p-toluenesulfonate.

In another embodiment, in p-toluenesulfonate of compound I, the molar ratio of compound I and p-toluenesulfonic acid is 1:1 or 2:1.

In another embodiment, the solvate is methanol or ethanol solvate of the p-toluenesulfonate of compound I.

In another embodiment, the polymorph is polymorph I of the 1/1 p-toluenesulfonate of compound I (1:1), wherein polymorph I has 1 to 3 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.182±0.2°, 21.472±0.2° and 22.833±0.2°.

In another embodiment, polymorph I further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 4.397±0.2°, 16.636±0.2°, 17.821±0.2°, 20.407±0.2° and 20.782±0.2°.

In another embodiment, polymorph I has characteristic peaks in X-ray powder diffraction as essentially shown in FIG. 1 a.

In another embodiment, polymorph I has a maximum peak of 231.5-237.7° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph I has a differential scanning calorimetry pattern as essentially shown in FIG. 1 b.

In another embodiment, in polymorph I, the molar ratio of compound I and p-toluenesulfonic acid is 1:1.

In another embodiment, the polymorph is polymorph II of methanol solvate of the 1/1 p-toluenesulfonate of compound I (1:1:1), wherein polymorph II has 1 to 3 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 21.014±0.2°, 18.333±0.2° and 25.301±0.2°.

In another embodiment, polymorph II further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 8.405±0.2°, 15.906±0.2°, 19.477±0.2° and 24.744±0.2°.

In another embodiment, polymorph II has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 2 a.

In another embodiment, polymorph II has maximum peaks of 193.5-197.0° C. and 228.6-236.4° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph II of the methanol solvate has a differential scanning calorimetry pattern as essentially shown in FIG. 2 b.

In another embodiment, in polymorph II, the molar ratio of compound I, p-toluenesulfonic acid and methanol is 1:1:1.

In another embodiment, the polymorph is polymorph III of the 1/1 p-toluenesulfonate of compound I (1:1), wherein polymorph III has 1 or 2 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 19.858±0.2° and 25.896±0.2°.

In another embodiment, polymorph III further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 17.726±0.2°, 19.325±0.2° and 21.575±0.2°.

In another embodiment, polymorph III has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 3 a.

In another embodiment, polymorph III has maximum peaks of 193.8-197.2° C. and 231.3-236.9° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph III has a differential scanning calorimetry pattern as essentially shown in FIG. 3 b.

In another embodiment, in polymorph III, the molar ratio of compound I to p-toluenesulfonic acid is 1:1.

In another embodiment, the polymorph is polymorph IV of ethanol solvate of the 1/1 p-toluenesulfonate of compound I (1:1:1), wherein polymorph IV has 1 or 2 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 20.961±0.2° and 18.277±0.2°.

In another embodiment, polymorph IV further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 9.273±0.2°, 15.812±0.2°, 24.674±0.2°, 25.246±0.2° and 27.552±0.2°.

In another embodiment, polymorph IV has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 4 a.

In another embodiment, polymorph IV has maximum peaks of 190.8-192.5° C. and 230.0-237.4° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph IV has a differential scanning calorimetry pattern as essentially shown in FIG. 4 b.

In another embodiment, in polymorph IV, the molar ratio of compound I, p-toluenesulfonic acid and ethanol is 1:1:1.

In another embodiment, the polymorph is polymorph V of the 1/2 p-toluenesulfonate of compound I (2:1), wherein polymorph V has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.423±0.2°, 13.974±0.2°, 20.467±0.2°, 20.705±0.2°, 24.929±0.2° and 27.101±0.2°.

In another embodiment, polymorph V further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 17.192±0.2°, 19.778±0.2°, 22.799±0.2°, 23.590±0.2° and 27.416±0.2°.

In another embodiment, polymorph V has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 5 a.

In another embodiment, polymorph V has a maximum peak of 130-142.3° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph V has a differential scanning calorimetry pattern as essentially shown in FIG. 5 b.

In another embodiment, in polymorph V, the molar ratio of compound I top-toluenesulfonic acid is 2:1.

In another embodiment, the polymorph is polymorph VI of compound I, wherein polymorph VI has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 23.818±0.2°, 24.236±0.2°, 26.382±0.2°, 26.817±0.2°, 24.929±0.2° and 27.101±0.2°.

In another embodiment, polymorph VI further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 11.327±0.2°, 17.997±0.2°, 18.528±0.2° and 21.669±0.2°.

In another embodiment, polymorph VI has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 6 a.

In another embodiment, polymorph VI has a maximum peak of 211.5-213.6° C. in differential scanning calorimetry pattern.

In another embodiment, polymorph VI has a differential scanning calorimetry pattern as essentially shown in FIG. 6 b.

In the second aspect, it provides a use of the polymorphs of the first aspect of the present invention in preparation of a pharmaceutical composition for inhibiting phosphokinase (such as raf kinase).

In another embodiment, the pharmaceutical composition is used for treating or preventing cancer.

In the third aspect, a pharmaceutical composition is provided, wherein the composition comprises:

(a) the polymorph of the first aspect of the present invention; and

(b) a pharmaceutically acceptable carrier.

In the fourth aspect, a method for preparing the polymorphs of the first aspect of the present invention is provided, comprising a step of: forming salt of compound I with an acid and crystallizing in an inert solvent, or recrystallizing compound I or pharmaceutically acceptable salts thereof or solvates thereof in an inert solvent, thereby obtaining the polymorphs of the first aspect of the present invention.

In another embodiment, the acid is p-toluenesulfonic acid.

In another embodiment, the method for preparing polymorph I comprises a step of: in an inert solvent, recrystallizing compound I with p-toluenesulfonic acid, thereby obtaining the polymorph I of the present invention.

In another embodiment, the method for preparing polymorph II comprises a step of: in methanol, recrystallizing the polymorph I obtained in the aforesaid step, thereby obtaining the polymorph II of the present invention.

In another embodiment, the method for preparing polymorph III comprises a step of: drying the polymorph II obtained in the aforesaid step for a period, thereby obtaining the polymorph III of the present invention.

In another embodiment, the method for preparing polymorph IV comprises a step of: in ethanol, recrystallizing the polymorph I obtained in the aforesaid step, thereby obtaining the polymorph IV of the present invention.

In another embodiment, the method for preparing polymorph V comprises a step of: drying the polymorph I obtained in the aforesaid step for a period, thereby obtaining the polymorph V of the present invention.

It should be understood that in the present invention, any of the technical features specifically described above and below (such as in the Examples) can be combined with each other, thereby constituting new or preferred technical solutions which will not redundantly be described one by one herein.

DESCRIPTION OF FIGURES

FIG. 1 a shows an X-ray powder diffraction pattern of polymorph I of Example 1.

FIG. 1 b shows a differential scanning calorimetry pattern of polymorph I of Example 1.

FIG. 1 c shows a ¹H NMR pattern of polymorph I of Example 1.

FIG. 2 a shows an X-ray powder diffraction pattern of polymorph II of Example 2.

FIG. 2 b shows a differential scanning calorimetry pattern of polymorph II of Example 2.

FIG. 2 c shows a ¹H NMR pattern of polymorph II of Example 2.

FIG. 3 a shows an X-ray powder diffraction pattern of polymorph III of Example 3.

FIG. 3 b shows a differential scanning calorimetry pattern of polymorph III of Example 3.

FIG. 3 c shows a ¹H NMR pattern of polymorph III of Example 3.

FIG. 4 a shows an X-ray powder diffraction pattern of polymorph IV of Example 4.

FIG. 4 b shows a differential scanning calorimetry pattern of polymorph IV of Example 4.

FIG. 4 c shows a ¹H NMR pattern of polymorph IV of Example 4.

FIG. 5 a shows an X-ray powder diffraction pattern of polymorph V of Example 5.

FIG. 5 b shows a differential scanning calorimetry pattern of polymorph V of Example 5.

FIG. 5 c shows a ¹H NMR pattern of polymorph V of Example 5.

FIG. 6 a shows an X-ray powder diffraction pattern of polymorph VI of Example 6.

FIG. 6 b shows a differential scanning calorimetry pattern of polymorph VI of Example 6.

FIG. 6 c shows a ¹H NMR pattern of polymorph VI of Example 6.

FIG. 7 a shows an X-ray powder diffraction pattern of amorphous form of the p-toluenesulfonate of compound I.

FIG. 7 b shows a differential scanning calorimetry pattern of amorphous form of the p-toluenesulfonate of compound I.

FIG. 7 c shows a ¹H NMR pattern of amorphous form of the p-toluenesulfonate of compound I.

DETAILED DESCRIPTION OF INVENTION

After intensive studies for a long time, the inventors have unexpectedly discovered various polymorphs of compound I or pharmaceutically acceptable salts thereof, or solvates thereof, which are highly pure, very stable, and suitable for preparing pharmaceutical compositions inhibiting phosphokinase (such as raf kinase). Therefore, they are more beneficial for treating diseases such as cancer. Moreover, the polymorphs of the present invention are not prone to floating in the manufacturing process (such as subpackaging) of a drug, easy for collection so that it is easy to avoid wasting and it is helpful to protect the health of operators. Based on this discovery, the inventors have completed the present invention.

As used herein, “Compound of Formula I (or compound I)” refers to 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N— 1′,1′,1′-trideutero-methyl)picolinamide as shown by Formula I.

p-Toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

The p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide of the present invention comprises various forms of the p-toluenesulfonate of compound I.

Preferably, it is the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N— 1′,1′,1′-trideutero-methyl)picolinamide, which refers to a salt wherein the ratio of compound I and p-toluenesulfonic acid is 1:1; or the 1/2 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide, which refers to a salt wherein the ratio of compound I and p-toluenesulfonic acid is 2:1.

Polymorph

Solid exists in either an amorphous form or a crystal form. In the case of crystal form, the molecules orient in lattice sites of a 3D lattice. When a compound is crystallized from a solution or slurry, it can have various crystalline phases that have different arrangements and/or conformations of the molecules which called as “polymorphism”. Different polymorphs of a given substance may be different from each other in one or more physical properties, such as solubility and dissolution rate, true specific gravity, crystal form, accumulation mode, liquidity and/or solid state stability, and so on.

Crystallization

The production-scale crystallization can be achieved by operating a solution so as to exceed the solubility limit of a compound interested. This can be accomplished through a variety of methods, for example, dissolving a compound at a relatively high temperature, and then cooling the solution below a saturation limit, or reducing the liquid volume by boiling, atmospheric evaporation, vacuum drying or some other methods, or reducing the solubility of the interested compound by adding antisolvent or solvents with low solubility of the compound, or a mixture of such solvents. An alternative method is to reduce the solubility by adjusting the pH value. See Crystallization, Third Edition, J W Mullens, Butterworth-Heineman Ltd., 1993, ISBN 0750611294 for a detailed description of crystallization.

If formation of a salt and its crystallization are desired to occur simultaneously, and the solubility of salt is lower than the raw material in the reaction medium, then the salt can be crystallized directly by adding an appropriate acid or base. Similarly, in a medium in which the solubility of the desired final form is lower than that of reactant, the final product can directly crystallize when the synthetic reaction is completed.

Optimization of crystallization may include adding the crystal desired as a seed crystal in the crystallization medium. In addition, many crystallization methods use a combination of the above strategies. One way comprises: dissolving the interested compound in a solvent, then adding an antisolvent in an appropriate volume through a controlled mode, in order to make the system just below the saturation level. At this moment, the desired crystal seed may be added (the integrity of the seed is kept), then crystallization is achieved by cooling the system.

As used herein, the term “room temperature” generally refers to 4-30° C., preferably, 20±5° C.

Polymorph of the Present Invention

As used herein, the term “polymorphs of the present invention” comprises polymorphs of compound I or pharmaceutically acceptable salts thereof (such as the p-toluenesulfonate), or solvates thereof, and further comprises various polymorphs of a certain p-toluenesulfonate or solvates thereof.

The preferable polymorphs of the present invention include but are not limited to:

polymorph VI of compound I;

polymorph I or polymorph III of the 1/1 p-toluenesulfonate of compound I;

polymorph II of methanol solvate of the 1/1 p-toluenesulfonate of compound I or polymorph IV of ethanol solvate of the 1/1 p-toluenesulfonate of compound I; wherein, in polymorph II, the molar ratio of compound I, p-toluenesulfonic acid and methanol is 1:1:1; and in polymorph IV, the molar ratio of compound I, p-toluenesulfonic acid and ethanol is 1:1:1; and

polymorph V of the 1/2 p-toluenesulfonate of compound I.

Identification and Property of Polymorph

After preparing polymorphs of the p-toluenesulfonate of compound I, the property thereof is studied using various methods and instruments.

X-Ray Powder Diffraction

The method of X-ray powder diffraction determining crystal form is known in the field. For example, the pattern is obtained using copper radiation on X-ray powder diffractometer of Rigaku D/max 2550VB/PC, at a scanning rate of 2° per minute.

The polymorphs of the p-toluenesulfonate of compound I have a specific crystal form and specific characteristic peaks in X-ray powder diffraction pattern. The preferred embodiments include:

(1) Polymorph I

Polymorph I has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.182±0.2°, 21.472±0.2° and 22.833±0.2°. In another embodiment, polymorph I further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 4.397±0.2°, 16.636±0.2°, 17.821±0.2°, 20.407±0.2° and 20.782±0.2°. In another embodiment, polymorph I has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 1 a.

(2) Polymorph II

Polymorph II has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 21.014±0.2°, 18.333±0.2° and 25.301±0.2°. In another embodiment, polymorph II further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 8.405±0.2°, 15.906±0.2°, 19.477±0.2° and 24.744±0.2°. In another embodiment, polymorph II has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 2 a.

(3) Polymorph III

Polymorph III has 1 or 2 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 19.858±0.2° and 25.896±0.2°. In another embodiment, polymorph III further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 17.726±0.2°, 19.325±0.2° and 21.575±0.2°. In another embodiment, polymorph III has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 3 a.

(4) Polymorph IV

Polymorph IV has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 20.961±0.2° and 18.277±0.2°. In another embodiment, polymorph IV further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 9.273±0.2°, 15.812±0.2°, 24.674±0.2°, 25.246±0.2° and 27.552±0.2°. In another embodiment, polymorph IV has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 4 a.

(5) Polymorph V

Polymorph V has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.423±0.2°, 13.974±0.2°, 20.467±0.2°, 20.705±0.2°, 24.929±0.2° and 27.101±0.2°. In another embodiment, polymorph V further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 17.192±0.2°, 19.778±0.2°, 22.799±0.2°, 23.590±0.2° and 27.416±0.2°. In another embodiment, polymorph V has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 5 a.

(6) Polymorph VI

Polymorph VI has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 23.818±0.2°, 24.236±0.2°, 26.382±0.2°, 26.817±0.2°, 24.929±0.2° and 27.101±0.2°. In another embodiment, polymorph VI further has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 11.327±0.2°, 17.997±0.2°, 18.528±0.2° and 21.669±0.2°. In another embodiment, polymorph VI has characteristic peaks in X-ray powder diffraction pattern as essentially shown in FIG. 6 a.

Differential Scanning Calorimetry

Differential scanning calorimetry or DSC refers to a thermoanalytical technique in which the difference in the amount of energy required to increase the temperature of a sample and reference is measured as a function of temperature. Position, shape and number of peaks in DSC pattern are relevant to the properties of substance, so they can be used to identify a substance qualitatively. Generally, this method is use to detect phase transition temperature, glass transition temperature, reaction calorimetry and other parameters of a substance.

The method of DSC is known in the art. For example, differential scanning calorimeter of NETZSCH DSC 204 F1 can be used, at a heating rate of 10 degrees per minute, from 25° C. to 250° C., to obtain a DSC pattern of a crystal form.

The polymorphs of the p-toluenesulfonate of compound I have specific characteristic peaks in Differential Scanning calorimetry (DSC) pattern. Preferably, they are shown as follows:

(1) Polymorph I

Polymorph I has a maximum peak of 231.5-237.7° C. in DSC pattern. In another embodiment, polymorph I has a DSC pattern as essentially shown in FIG. 1 b.

(2) Polymorph II

Polymorph II has maximum peaks of 193.5-197.0° C. and 228.6-236.4° C. in DSC pattern. In another embodiment, polymorph II has a DSC pattern as essentially shown in FIG. 2 b.

(3) Polymorph III

Polymorph III has maximum peaks of 193.8-197.2° C. and 231.3-236.9° C. in DSC pattern. In another embodiment, polymorph III has a DSC pattern as essentially shown in FIG. 3 b.

(4) Polymorph IV

Polymorph IV has maximum peaks of 190.8-192.5° C. and 230.0-237.4° C. in DSC pattern. In another embodiment, polymorph IV has a DSC pattern as essentially shown in FIG. 4 b.

(5) Polymorph V

Polymorph V has a maximum peak of 130-142.3° C. in DSC pattern. In another embodiment, polymorph V has a DSC pattern as essentially shown in FIG. 5 b.

(6) Polymorph VI

Polymorph VI has a maximum peak of 211.5-213.6° C. in DSC pattern. In another embodiment, polymorph VI has a DSC pattern as essentially shown in FIG. 6 b.

Nuclear magnetic resonance (NMR) may further be used to assistantly determine the crystal structure. The detecting methods and instruments are known in the art, for example, one can use Bruker Avance III plus-400 MHz.

Active Ingredients

As used herein, the term “active ingredients” or “active compound” refers to the polymorphs of the present invention, i.e. polymorphs of compound I or pharmaceutically acceptable salts thereof (such as the p-toluenesulfonate), or solvates thereof.

Pharmaceutical Composition and the Administration Thereof

The polymorphs of the present invention possess outstanding activity of inhibiting phosphokinases, such as raf kinases. Therefore, the polymorphs of the present invention and the pharmaceutical composition comprising polymorphs of the present invention as a main active ingredient can be used for treating, preventing and alleviating diseases mediated by phosphokinases (e.g. raf kinase). Based on the prior art, the compounds of the invention can treat the following diseases: cancer, cardiovascular diseases, obesity, diabetes etc.

The pharmaceutical composition of the invention comprises the polymorph of the present invention in a safe and effective dosage range and pharmaceutically acceptable excipients or carriers.

Wherein, the term “safe and effective dosage” refers to the amount of the compounds (or the polymorphs) which is enough to improve the patient's condition without any serious side effect. Generally, the pharmaceutical composition contains 1-2000 mg polymorphs of the invention per dose, preferably, 10-200 mg polymorphs of the invention per dose. Preferably, “per dose” means one capsule or tablet.

“Pharmaceutically acceptable carrier” means one or more compatible solid or liquid fillers or gel materials, which are suitable for human, and must have sufficient purity and sufficiently low toxicity. “Compatibility” herein means that the components of the compositions can be blended with the compounds of the invention or with each other, and would not significantly reduce the efficacy of the compounds. Some examples of pharmaceutically acceptable carriers include cellulose and the derivatives thereof (such as sodium carboxymethyl cellulose, sodium ethyl cellulose, cellulose acetate, etc.), gelatin, talc, solid lubricants (such as stearic acid, magnesium stearate), calcium sulfate, vegetable oils (such as soybean oil, sesame oil, peanut oil, olive oil, etc.), polyols (such as propylene glycol, glycerol, mannitol, sorbitol, etc.), emulsifiers (such as Tween®), wetting agent (such as sodium dodecyl sulfate), coloring agents, flavoring agents, stabilizers, antioxidants, preservatives, pyrogen-free water, etc.

There is no special limitation of administration mode for the polymorphs or pharmaceutical compositions of the present invention, and the representative administration mode includes (but is not limited to): oral, intratumoral, rectal, parenteral (intravenous, intramuscular or subcutaneous), and topical administration.

Solid dosage forms for oral administration include capsules, tablets, pills, powders and granules. In these solid dosage forms, the active ingredients are mixed with at least one conventional inert excipient (or carrier), such as sodium citrate or CaHPO₄, or mixed with any of the following components: (a) fillers or compatibilizer, for example, starch, lactose, sucrose, glucose, mannitol and silicic acid; (b) binders, for example, hydroxymethyl cellulose, alginates, gelatin, polyvinylpyrrolidone, sucrose and arabic gum; (c) humectant, such as, glycerol; (d) disintegrating agents such as agar, calcium carbonate, potato starch or tapioca starch, alginic acid, certain composite silicates, and sodium carbonate; (e) dissolution-retarding agents, such as paraffin; (f) absorption accelerators, for example, quaternary ammonium compounds; (g) wetting agents, such as cetyl alcohol and glyceryl monostearate; (h) adsorbents, for example, kaolin; and (i) lubricants such as talc, stearin calcium, magnesium stearate, solid polyethylene glycol, sodium lauryl sulfate, or the mixtures thereof. In capsules, tablets and pills, the dosage forms may also contain buffering agents.

The solid dosage forms such as tablets, sugar pills, capsules, pills and granules can be prepared by using coating and shell materials, such as enteric coatings and any other materials known in the art. They can contain a opaque agent. The release of the active compounds or compounds in the compositions can be released in a delayed mode in a given portion of the digestive tract. Examples of the embedding components include polymers and waxes. If necessary, the active compounds and one or more above excipients can form microcapsules.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups or tinctures. In addition to the active ingredients, the liquid dosage forms may contain any conventional inert diluents known in the art such as water or other solvents, solubilizers and emulsifiers, for example, ethanol, isopropanol, ethyl carbonate, ethyl acetate, propylene glycol, 1,3-butanediol, dimethyl formamide, as well as oil, in particular, cottonseed oil, peanut oil, corn germ oil, olive oil, castor oil and sesame oil, or the combination thereof.

Besides these inert diluents, the composition may also contain additives such as wetting agents, emulsifiers, and suspending agent, sweetener, flavoring agents and perfume.

In addition to the active ingredients, the suspension may contain suspending agent, for example, ethoxylated isooctadecanol, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, methanol aluminum and agar, or the combination thereof.

The compositions for parenteral injection may comprise physiologically acceptable sterile aqueous or anhydrous solutions, dispersions, suspensions or emulsions, and sterile powders which can be re-dissolved into sterile injectable solutions or dispersions. Suitable aqueous and non-aqueous carriers, diluents, solvents or excipients include water, ethanol, polyols and any suitable mixtures thereof.

The dosage forms for topical administration of compounds of the invention include ointments, powders, patches, aerosol, and inhalants. The active ingredients are mixed with physiologically acceptable carriers and any preservatives, buffers, or propellant if necessary, under sterile conditions.

Polymorphs of the present invention can be administrated alone, or in combination with any other pharmaceutically acceptable compounds.

When the pharmaceutical compositions are used, a safe and effective amount of polymorph of the present invention is applied to a mammal (such as human) in need of, wherein the dose of administration is a pharmaceutically effective dose. For a person weighed 60 kg, the daily dose is usually 1-2000 mg, preferably 20-500 mg. Of course, the particular dose should also depend on various factors, such as the route of administration, patient healthy status, which are well within the skills of an experienced physician.

The main advantages of the present invention are:

1. a series of novel polymorphs of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide or salts thereof, or solvates thereof are provided, including polymorphs I to VI;

2. a use of various polymorphs in preparing a pharmaceutical composition useful for inhibiting phosphokinase (such as raf kinase) is provided.

The present invention will be further illustrated below with reference to the specific examples. It should be understood that these examples are only to illustrate the invention but not to limit the scope of the invention. The experimental methods with no specific conditions described in the following examples are generally performed under the conventional conditions, or according to the manufacture's instructions. Unless indicated otherwise, parts and percentage are calculated by weight.

Example 1 Polymorph I of the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

50 g of methyl 4-chloro-2-picolinate was dissolved in 250 mL of tetrahydrofuran in a three-necked flask, then 31 g of deuterated methylamine hydrochloride and 80 g of anhydrous potassium carbonate were added respectively. After the mixture was stirred at 25° C. for 20 hours, 250 mL of water and 100 mL of methyl tert-butyl ether were added. The mixture was stirred and separated, and the aqueous phase was extracted with 100 mL of methyl tert-butyl ether. The organic phases were combined and dried, and the solvent was removed under reduced pressure to give 48 g of pale yellow liquid.

The pale yellow liquid was dissolved in 50 mL of dimethylsulfoxide, then 30 g of 4-aminophenol was added and 31 g of potassium t-butoxide was added in portions. The mixture was heated to 80° C. and stirred for 4 hours. 100 mL of hydrochloric acid was added dropwise, then the mixture was filtered and the filter cake was suspended in 150 mL of acetone. The suspension was stirred at 25° C. for 16 hours and filtered. The filter cake was dissolved in 100 mL of water, and extracted with 200 mL of ethyl acetate twice. The organic phase was dried, and the solvent was removed under reduced pressure to obtain 51 g of light brown solid.

The resultant light brown solid was dissolved in 50 mL of N,N-dimethylformamide. A solution of 4-chloro-3-trifluoromethylphenyl isocyanate (48 g) in ethyl acetate (50 mL) was added dropwise, and the mixture was stirred at 25° C. for 2 hours. Then 130 mL of water was added dropwise, and the mixture was stirred for 1 hour, filtered and dried to give 77 g of pale yellow solid, i.e., 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide.

45 g of pale yellow solid was added into 450 mL of tetrahydrofuran, then 6.6 g of p-toluenesulfonic acid monohydrate was added. The mixture was heated to reflux until the solution was clear. After hot filtration, the filtrate was re-heated to reflux until the solution was clear, then a solution of p-toluenesulfonic acid monohydrate (16.1 g) in tetrahydrofuran (50 mL) at 70° C. was flowed into the above clear solution rapidly. Keep the temperature for 30 minutes, then stop heating and cool to 0° C. The mixture was filtered, and the filter cake was taken out and dried under vacuum for 24 hours at room temperature to constant weight to give 55.2 g of the title compound.

NMR data showed that the molar ratio of compound I and p-toluenesulfonic acid was 1:1.

¹H NMR (DMSO-d6, 400 MHz): δ 2.30 (s, 3H), 7.15 (d, J=8.8 Hz, 2H), 7.20 (d, J=8.8 Hz, 2H), 7.23 (dd, J=2.8 Hz, 6 Hz, 1H), 7.52 (d, J=8 Hz, 2H), 7.55 (d, J=2.8 Hz, 1H), 7.63 (d, J=8.8 Hz, 3H), 7.68 (dd, J=2.4 Hz, 9.2 Hz, 1H), 8.03 (br, 1H), 8.14 (d, J=2.4 Hz, 1H), 8.56 (d, J=6 Hz, 1H), 8.91 (br, 1H), 9.17 (br, 1H), 9.36 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 1 a, parameters of each peak are shown in Table 1, the differential scanning calorimetry pattern (DSC) is shown in FIG. 1 b, and ¹H NMR is shown in FIG. 1 c.

TABLE 1 Peak relative intensity No. 2θ(°) Height (I %) 1 4.397 9535 59.02 2 10.643 1136 7.03 3 11.068 2874 17.79 4 11.608 1178 7.29 5 12.193 1266 7.84 6 12.791 2601 16.10 7 13.182 16155 100.00 8 14.759 5166 31.98 9 15.981 1603 9.92 10 16.636 7569 46.85 11 17.821 9542 59.07 12 18.764 4001 24.77 13 19.360 3516 21.76 14 20.030 5597 34.65 15 20.407 9135 56.55 16 20.782 8830 54.66 17 21.472 12236 75.74 18 22.076 1648 10.20 19 22.833 11201 69.33 20 23.345 3025 18.72 21 23.640 2644 16.37 22 24.472 3676 22.75 23 25.005 3472 21.49 24 25.355 2040 12.63 25 25.968 2673 16.55 26 26.578 2632 16.29 27 26.917 1622 10.04 28 27.292 1631 10.10 29 28.101 1845 11.42 30 28.535 2569 15.90 31 29.524 2219 13.74 32 29.837 1865 11.54 33 30.785 2058 12.74 34 31.084 1812 11.22 35 31.538 1674 10.36 36 31.974 1364 8.44 37 33.169 1275 7.89 38 33.863 1677 10.38 39 34.180 1580 9.78 40 35.695 1035 6.41 41 37.021 941 5.82 42 38.420 899 5.56 43 39.213 1352 8.37 44 41.124 1354 8.38

Example 2 Polymorph II of methanol solvate of the 1/1 p-toluenesulfonate of

4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide (The molar ratio of compound I, p-toluenesulfonic acid and methanol is 1:1:1) 10 g of polymorph I prepared in Example 1 was added into 100 g of methanol. The mixture was heated to reflux until the solution was clear, then a solution of p-toluenesulfonic acid monohydrate (6.1 g) in methanol (25 g) was added dropwise. The mixture was cooled to 30° C. naturally after it was clear, and then stirred for 1.5 hours, and filtered. The filter cake was taken out, dried under vacuum at room temperature to constant weight to give 12 g of white solid, which was sampled and characterized through ¹H NMR, X-ray powder diffraction, DSC, etc., demonstrating that the title compound was obtained.

NMR data showed that the molar ratio of compound I, p-toluenesulfonic acid and methanol was 1:1:1.

¹H NMR (DMSO-d6, 400 MHz): δ2.29 (s, 3H), 3.17 (s, 3H), 7.14 (d, J=8 Hz, 2H), 7.20 (d, J=8.2 Hz, 2H), 7.24 (dd, J=2.4 Hz, 6 Hz, 1H), 7.52 (d, J=8 Hz, 2H), 7.57-7.69 (m, 5H), 8.13 (d, J=2 Hz, 1H), 8.38 (br, 1H), 8.56 (d, J=6.4 Hz, 1H), 8.95 (br, 1H), 9.20 (br, 1H), 9.39 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 2 a, parameters of each peak are shown in Table 2, the differential scanning calorimetry pattern (DSC) is shown in FIG. 2 b, and ¹H NMR is shown in FIG. 2 c.

TABLE 2 Peak relative intensity No. 2θ(°) Height (I %) 1 7.996 3315 7.45 2 8.405 9975 22.41 3 9.370 5972 13.42 4 12.214 3052 6.86 5 13.085 2009 4.51 6 13.460 2179 4.90 7 15.906 10390 23.34 8 16.988 1079 2.42 9 17.777 1790 4.02 10 18.333 17222 38.70 11 19.020 4626 10.39 12 19.477 8049 18.08 13 20.281 1939 4.36 14 20.526 3444 7.74 15 21.014 44507 100.00 16 21.768 4833 10.86 17 22.477 5721 12.85 18 23.897 2109 4.74 19 24.744 10801 24.27 20 25.301 21550 48.42 21 25.730 3443 7.74 22 26.034 2925 6.57 23 26.957 6747 15.16 24 27.627 8140 18.29 25 28.416 2063 4.64 26 28.889 6042 13.58 27 29.165 3503 7.87 28 29.760 4274 9.60 29 30.270 1810 4.07 30 30.943 1966 4.42 31 31.494 2442 5.49 32 32.009 2651 5.96 33 33.017 2159 4.85 34 33.430 1923 4.32 35 34.181 1137 2.55 36 34.616 1512 3.40 37 37.281 1305 2.93 38 40.301 1345 3.02

Example 3 Polymorph III of the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

2 g of polymorph II prepared in example 2 was dried in a vacuum oven at 85° C. for 20 hours to constant weight, which was sampled and determined through ¹H NMR, X-ray powder diffraction, DSC, etc. The results demonstrated the title compound (1.85 g) was obtained.

NMR data showed that the molar ratio of compound I and p-toluenesulfonic acid was 1:1.

¹H NMR (DMSO-d6, 400 MHz): δ2.29 (s, 3H), 3.17 (s, 3H), 7.13 (d, J=8 Hz, 2H), 7.19 (d, J=9.2 Hz, 2H), 7.22 (dd, J=2.4 Hz, 6 Hz, 1H), 7.50-7.53 (m, 3H), 7.60-7.69 (m, 4H), 8.13 (d, J=2.4 Hz, 1H), 8.38 (br, 1H), 8.55 (d, J=5.6 Hz, 1H), 8.90 (br, 1H), 9.15 (br, 1H), 9.35 (br, 1H), 9.63 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 3 a, parameters of each peak are shown in Table 3, the differential scanning calorimetry diagram (DSC) is shown in FIG. 3 b, and ¹H NMR is shown in FIG. 3 c.

TABLE 3 Peak relative intensity No. 2θ(°) Height (I %) 1 7.676 723 5.55 2 8.546 1575 12.09 3 9.773 725 5.57 4 10.617 1144 8.78 5 11.982 2421 18.59 6 12.319 740 5.68 7 12.926 943 7.24 8 13.382 765 5.87 9 16.029 1892 14.53 10 17.193 2155 16.55 11 17.726 4749 36.47 12 18.792 1831 14.06 13 19.325 4336 33.29 14 19.858 13023 100.00 15 20.270 3203 24.59 16 20.826 2077 15.95 17 21.575 6037 46.36 18 22.483 1970 15.13 19 22.936 1186 9.11 20 23.370 1159 8.90 21 24.198 3194 24.53 22 24.834 1112 8.54 23 25.896 7377 56.65 24 26.864 1270 9.75 25 27.692 3058 23.48 26 28.149 1833 14.08 27 29.392 1911 14.67 28 29.787 2386 18.32 29 31.443 1557 11.96 30 32.175 1260 9.68 31 33.459 638 4.90 32 34.085 817 6.27 33 35.212 860 6.60 34 36.140 710 5.45 35 37.229 608 4.67 36 39.557 604 4.64 37 40.567 579 4.45 38 41.135 582 4.47 39 43.382 670 5.14 40 43.877 655 5.03

Example 4 polymorph IV of ethanol solvate of the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide (molar ratio of the compound of formula I, p-toluenesulfonic acid and ethanol is 1:1:1)

5 g of polymorph I prepared in example 1 was suspended in 20 ml of ethanol. The mixture was stirred at room temperature for 16 hours, and filtered. The filter cake out was taken out and dried in vacuo at room temperature for 20 hours to constant weight to give 4.8 g of pale yellow solid, which was sampled and determined through ¹H NMR, X-ray powder diffraction, DSC, etc., demonstrating that the title compound was obtained.

NMR data showed that the molar ratio of compound I, p-toluenesulfonic acid and ethanol was 1:1:1.

¹H NMR (DMSO-d6, 400 MHz): δ1.05 (1, J=6.8 Hz, 3H), 2.29 (s, 3H), 3.44 (q, J=7.2 Hz, 2H), 7.13 (d, J=7.6 Hz, 2H), 7.19 (d, J=8.8 Hz, 2H), 7.22 (dd, J=2.8 Hz, 6 Hz, 1H), 7.51 (d, J=8.4 Hz, 2H), 7.54 (d, J=2.8 Hz, 1H), 7.60-7.69 (m, 4H), 7.97 (br, 1H), 8.13 (d, J=2.4 Hz, 1H), 8.55 (d, J=6 Hz, 1H), 8.92 (br, 1H), 9.16 (br, 1H), 9.36 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 4 a, parameters of each peak are shown in Table 4, the differential scanning calorimetry pattern (DSC) is shown in FIG. 4 b, and ¹H NMR is shown in FIG. 4 c.

TABLE 4 Peak relative intensity No. 2θ(°) Height (I %) 1 7.915 1966 17.64 2 8.386 1884 16.90 3 9.273 4236 38.00 4 9.534 786 7.05 5 11.186 741 6.65 6 11.976 2299 20.63 7 12.178 919 8.25 8 12.827 1362 12.22 9 13.417 711 6.38 10 15.812 3239 29.06 11 16.759 756 6.78 12 18.277 7399 66.38 13 18.832 2363 21.20 14 19.400 2656 23.83 15 19.954 813 7.29 16 20.414 1075 9.64 17 20.961 11146 100.00 18 21.456 2214 19.86 19 21.706 851 7.64 20 22.422 1986 17.82 21 23.786 1173 10.52 22 24.674 3954 35.47 23 25.246 4011 35.99 24 25.898 1159 10.40 25 26.353 1382 12.40 26 26.922 1896 17.01 27 27.552 3263 29.28 28 28.323 1168 10.48 29 28.818 2862 25.68 30 29.111 996 8.94 31 29.646 1226 11.00 32 30.378 920 8.25 33 30.872 1403 12.59 34 31.364 752 6.75 35 31.954 1151 10.33 36 32.924 1194 10.71 37 33.876 685 6.15 38 34.523 753 6.76 39 36.578 611 5.48 40 37.030 566 5.08 41 40.171 754 6.76 42 41.809 644 5.78 43 42.673 551 4.94 44 43.957 630 5.65

Example 5 Polymorph V of the 1/2 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

3 g of polymorph I prepared in example 1 was suspended in 50 ml of water. The mixture was stirred at room temperature for 24 hours, and filtered. The filter cake was taken out and dried in vacuo at room temperature for 48 hours, which was sampled and determined through ¹H NMR, X-ray powder diffraction, DSC, etc., demonstrating that 1.2 g of title compound was obtained.

NMR data showed that the molar ratio of compound I and p-toluenesulfonic acid was 2:1.

¹H NMR (DMSO-d6, 400 MHz): δ2.29 (s, 1.5H), 7.13 (d, J=8 Hz, 1H), 7.17-7.20 (m, 3H), 7.46 (d, J=2.4 Hz, 1H), 7.51 (d, J=8 Hz, 2H), 7.60-7.66 (m, 4H), 8.13 (d, J=2.4 Hz, 1H), 8.53 (d, J=6 Hz, 1H), 8.84 (br, 1H), 9.09 (br, 1H), 9.29 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 5 a, parameters of each peak are shown in Table 5, the differential scanning calorimetry diagram (DSC) is shown in FIG. 5 b, and ¹H NMR is shown in FIG. 5 c.

TABLE 5 Peak relative intensity No. 2θ(°) Height (I %) 1 5.570 779 12.17 2 6.611 1161 18.13 3 8.010 959 14.98 4 9.017 3356 52.42 5 9.595 2872 44.86 6 9.869 2591 40.47 7 10.601 1063 16.60 8 10.914 1625 25.38 9 11.207 1266 19.78 10 11.891 814 12.71 11 12.749 1053 16.45 12 13.423 5460 85.29 13 13.974 6003 93.77 14 14.530 1645 25.70 15 15.019 1178 18.40 16 15.709 2621 40.94 17 16.108 1667 26.04 18 16.578 3549 55.44 19 16.757 3439 53.72 20 17.192 4282 66.89 21 18.320 3397 53.06 22 18.911 2251 35.16 23 19.283 2641 41.25 24 19.778 4064 63.48 25 20.467 5269 82.30 26 20.705 4945 77.24 27 21.003 1656 25.87 28 21.455 3511 54.84 29 22.000 1110 17.34 30 22.341 1770 27.65 31 22.799 3980 62.17 32 23.314 2515 39.28 33 23.590 4436 69.29 34 24.159 3616 56.48 35 24.929 6402 100.00 36 25.503 2651 41.41 37 25.721 3267 51.03 38 26.149 1873 29.26 39 27.101 5429 84.80 40 27.416 4202 65.64 41 28.265 2716 42.42 42 28.599 1432 22.37 43 29.133 1490 23.27 44 29.826 1737 27.13 45 30.282 1282 20.02 46 31.185 1473 23.01 47 31.625 1087 16.98 48 32.666 1453 22.70 49 33.551 1282 20.02 50 34.030 1512 23.62 51 34.781 1225 19.13 52 36.242 959 14.98 53 36.693 1297 20.26 54 37.308 965 15.07 55 37.722 933 14.57 56 38.155 974 15.21 57 38.845 1077 16.82 58 40.461 898 14.03 59 41.568 802 12.53 60 42.383 780 12.18 61 43.427 850 13.28

Example 6 polymorph VI of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

50 g of methyl 4-chloro-2-picolinate was dissolved in 250 mL of tetrahydrofuran in three-necked flask, then 31 g of deuterated methylamine hydrochloride and 80 g of anhydrous potassium carbonate were added respectively. After the mixture was stirred at 25° C. for 20 hours, 250 mL of water and 100 mL of methyl tert-butyl ether were added, The mixture was stirred and separated, and the aqueous phase was extracted with 100 mL of methyl tert-butyl ether. The organic phases were combined and dried, the solvent was removed under reduced pressure to give 48 g of pale yellow liquid.

The pale yellow liquid was dissolved in 50 mL of dimethylsulfoxide, 30 g of 4-aminophenol was added and 31 g of potassium t-butoxide was added in portions. The mixture was heated to 80° C. and stirred for 4 hours. 100 mL of hydrochloric acid was added dropwise, then the mixture was filtered and the filter cake was suspended in 150 mL of acetone. The suspension was stirred at 25° C. for 16 hours, and filtered. The filter cake was dissolved in 100 mL of water, and extracted with 200 mL of ethyl acetate twice. The organic phase was dried, and the solvent was removed under reduced pressure to obtain 51 g of light brown solid.

The resultant light brown solid was dissolved in 50 mL of N,N-dimethylformamide. A solution of 4-chloro-3-trifluoromethylphenyl isocyanate (48 g) in ethyl acetate (50 mL) was added dropwise, and the mixture was stirred at 25° C. for 2 hours. Then 130 mL of water was added dropwise, and the mixture was stirred for 1 hour, filtered and dried in vacuo at 25° C. for 24 hours to give a pale yellow solid, which was sampled and determined through ¹H NMR, X-ray powder diffraction, DSC, etc., demonstrating that the title compound (77g) was obtained.

¹H NMR (DMSO-d6, 400 MHz): δ7.15 (dd, J=2.8 Hz, 5.6 Hz, 1H), 7.17-7.19 (m, 2H), 7.40 (d, J=2.4 Hz, 1H), 7.59-7.69 (m, 4H), 8.13 (d, J=2.4 Hz, 1H), 8.51 (d, J=6 Hz, 1H), 8.75 (br, 1H), 8.90 (br, 1H), 9.22 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 6 a, parameters of each peak are shown in Table 6, the differential scanning calorimetry diagram (DSC) is shown in FIG. 6 b, and ¹H NMR is shown in FIG. 6 c.

TABLE 6 Peak relative intensity No. 2θ(°) Height (I %) 1 6.549 1062 2.18 2 9.806 2156 4.42 3 11.327 5816 11.94 4 12.490 17961 36.86 5 13.105 2458 5.04 6 13.496 3135 6.43 7 14.484 5096 10.46 8 15.037 4170 8.56 9 15.551 3156 6.48 10 16.257 1228 2.52 11 17.033 2348 4.82 12 17.997 4940 10.14 13 18.528 5423 11.13 14 18.985 4093 8.40 15 19.711 5440 11.16 16 21.669 3610 7.41 17 21.925 7892 16.20 18 22.379 14496 29.75 19 22.834 27515 56.47 20 23.465 4326 8.88 21 23.818 2862 5.87 22 24.236 5232 10.74 23 24.686 48724 100.00 24 25.105 33185 68.11 25 25.555 7452 15.29 26 26.382 3451 7.08 27 26.817 4602 9.45 28 28.002 1827 3.75 29 28.418 1641 3.37 30 29.561 4191 8.60 31 30.293 3754 7.70 32 31.514 2316 4.75 33 32.543 1872 3.84 34 32.779 1838 3.77 35 34.990 2317 4.76 36 36.390 2058 4.22 37 37.849 2329 4.78 38 38.779 1223 2.51 39 40.021 2093 4.30 40 41.149 1194 2.45 41 41.913 1084 2.22 42 42.784 1718 3.53

Example 7 Amorphous form of the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

0.5 g of polymorph I prepared in example 1 was suspended in 500 mL of ethanol. The mixture was heated under reflux until it was completely dissolved. The solvent was removed under reduced pressure at 80° C. using rotary evaporation, and the solid was dried in vacuo at 50° C. for 28 hours and milled to give a pale yellow powder, which was sampled and determined through ¹H NMR, X-ray powder diffraction, DSC, etc., demonstrating that 0.41 g of the title compound was obtained.

NMR data showed that the molar ratio of compound I and p-toluenesulfonic acid was 1:1.

¹H NMR (DMSO-d6, 400 MHz): δ2.30 (s, 3H), 7.15 (d, J=8.8 Hz, 2H), 7.20 (d, J=8.8 Hz, 2H), 7.23 (dd, J=2.8 Hz, 6 Hz, 1H), 7.52 (d, J=8 Hz, 2H), 7.55 (d, J=2.8 Hz, 1H), 7.63 (d, J=8.8 Hz, 3H), 7.68 (dd, J=2.4 Hz, 9.2 Hz, 1H), 8.03 (br, 1H), 8.14 (d, J=2.4 Hz, 1H), 8.56 (d, J=6 Hz, 1H), 8.91 (br, 1H), 9.17 (br, 1H), 9.36 (br, 1H).

The X-ray powder diffraction pattern is shown in FIG. 7 a, the differential scanning calorimetry pattern (DSC) is shown in FIG. 7 b, and ¹H NMR is shown in FIG. 7 c.

Example 8 Stability of polymorph I of the 1/1 p-toluenesulfonate of 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}-2-(N-1′,1′,1′-trideutero-methyl)picolinamide

After an accelerated stability test (test condition: 40° C., 75% RH) for 1-6 months, the results showed that: crystal form of polymorph I was very stable; compared to polymorph I freshly prepared (0 Months), the purity of polymorph I was almost unchanged, always above 99%.

Example 9 Pharmaceutical Composition

Polymorph I of the 1/1 p-toluenesulfonate of 20 g 4-(4-{3-[4-chloro-3-(trifluoromethyl)phenyl)-ureido]-phenoxy}- 2-(N-1′,1′,1′-trideutero-methyl)picolinamide (Example 1) Starch 140 g  Microcrystalline cellulose 60 g

According to the conventional method, the above materials were mixed and encapsulated into ordinary gelatin capsule to give 1,000 capsules.

Example 10 Drug Hygroscopicity Test

The test was performed according to the guiding principles of drug hygroscopic test (Chinese Pharmacopoeia 2010 edition, Appendix XIX J).

1. Take 4 dry glass weighing bottles with a top (The outer diameter was 60 mm and height was 30 mm) On the day before the test, the bottles was placed in a glass dryer (A saturated ammonium sulfate solution was placed in the lower part thereof) in a thermostatic and humidistatic chamber at 25° C.±1° C. (hereinafter, “a humidistatic dryer at 25° C.±1° C.”). The weighing bottle and its top were placed separately without the top on the bottle. Cover the glass dryer closely.

2. After each empty weighing bottle together with its top were placed in a humidistatic dryer at 25° C.±1° C. for 24 hours, weigh a set (the weighing bottle+its top) as a unit precisely respectively, recorded as m1. Take a sample appropriately, tile it in a glass weighing bottle weighed at a sample thickness of about 1 mm, and cover the bottle. Precisely weigh the weighing bottle with its top and the sample, recorded as m2. Put 4 kinds of salts of free alkali compound I (ZJCM03) in 4 weighing bottles respectively. Then take off the top of the weighing bottles, and put the bottle and its top in the humidistatic dryer at 25° C.±1° C. for 24 hours.

3. After each sample were placed in a humidistatic dryer at 25° C.±1° C. for 24 hours, cover the weighing bottles with their tops respectively, and precisely weigh each weighing bottle with its top and the sample at this specific moment, recorded as m3.

4. Calculate the weight increase (%) of each sample according to the following equation.

the weight increase(%)=[(m3−m2)/(m2−m1)]×100%

It is defined as no or almost no hygroscopicity when the weight increase (%) is less than 0.2%.

According to the above steps, the hygroscopicity of the polymorphs of the present invention was tested. The results showed that the weight increase (%) of polymorph I=[(39.951−39.951)/(39.951−38.836)]×100%=0. The result showed that polymorph I had no hygroscopicity.

Repeat Example 8 and Example 10 except that polymorphs II, III, IV, V or VI was used instead of polymorph I. The results showed that each polymorph of the present invention was very stable, had no or almost no hygroscopicity.

Therefore, polymorphs of the present invention are very suitable to be used in pharmaceutical compositions. Moreover, the polymorphs of the present invention, which are not prone to floating in the manufacturing process (such as subpackaging) of a drug and are easy for collection so that it is easy to avoid wasting and it is helpful to protect the health of operators.

All literatures mentioned in the present application are incorporated by reference herein, as though individually incorporated by reference. Additionally, it should be understood that after reading the above teaching, many variations and modifications may be made by the skilled in the art, and these equivalents also fall within the scope as defined by the appended claims. 

1. A polymorph of compound I or a pharmaceutically acceptable salt thereof or a solvate thereof,


2. The polymorph of claim 1, wherein the polymorph is polymorph I of the 1/1 p-toluenesulfonate of compound I, and polymorph I has 1 to 3 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.182±0.2°, 21.472±0.2° and 22.833±0.2°.
 3. The polymorph of claim 2, wherein polymorph I has a maximum peak of 231.5-237.7° C. in differential scanning calorimetry pattern.
 4. The polymorph of claim 1, wherein the polymorph is polymorph II of methanol solvate of the 1/1 p-toluenesulfonate of compound I (1:1:1), and polymorph II has 1 to 3 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 21.014±0.2°, 18.333±0.2° and 25.301±0.2°.
 5. The polymorph of claim 4, wherein polymorph II has maximum peaks of 193.5-197.0° C. and 228.6-236.4° C. in differential scanning calorimetry pattern.
 6. The polymorph of claim 1, wherein the polymorph is polymorph III of the 1/1 p-toluenesulfonate of compound I, and polymorph III has 1 or 2 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 19.858±0.2° and 25.896±0.2°.
 7. The polymorph of claim 6, wherein polymorph III has maximum peaks of 193.8-197.2° C. and 231.3-236.9° C. in differential scanning calorimetry pattern.
 8. The polymorph of claim 1, wherein the polymorph is polymorph IV of ethanol solvate of the 1/1 p-toluenesulfonate of compound I, and polymorph IV has 1 or 2 characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 20.961±0.2° and 18.277±0.2°.
 9. The polymorph of claim 8, wherein polymorph IV has maximum peaks of 190.8-192.5° C. and 230.0-237.4° C. in differential scanning calorimetry pattern.
 10. The polymorph of claim 1, wherein the polymorph is polymorph V of the 1/2 p-toluenesulfonate of compound I, and polymorph V has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 13.423±0.2°, 13.974±0.2°, 20.467±0.2°, 20.705±0.2°, 24.929±0.2° and 27.101±0.2°.
 11. The polymorph of claim 10, wherein polymorph V has a maximum peak of 130-142.3° C. in differential scanning calorimetry pattern.
 12. The polymorph of claim 1, wherein, the polymorph is polymorph VI of compound I, and polymorph VI has one or more characteristic peaks in X-ray powder diffraction pattern selected from the group consisting of 23.818±0.2°, 24.236±0.2°, 26.382±0.2°, 26.817±0.2°, 24.929±0.2° and 27.101±0.2°.
 13. The polymorph of claim 12, wherein, polymorph VI has a maximum peak of 211.5-213.6° C. in differential scanning calorimetry pattern. 14-15. (canceled)
 16. A pharmaceutical composition which comprises: (a) the polymorph of claim 1; and (b) a pharmaceutically acceptable carrier.
 17. A method for preparing the polymorph of claim 1, comprising a step of: forming salt of compound I with an acid and crystallizing in an inert solvent, or recrystallizing compound I and a pharmaceutically acceptable salt thereof or a solvate thereof in an inert solvent, thereby obtaining the polymorph of claim
 1. 18. A method of inhibiting phosphokinase in a subject in need thereof, comprising administering to the subject a pharmaceutical composition comprising an effective amount of the polymorph of claim
 1. 19. The method of claim 18, wherein the pharmaceutical composition treats or prevents a cancer in the subject. 